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Hydrochloric Acid → Ethyl 6-methylpiperidine-3-carboxylate

HRID 1019660
ノート
印刷プレビュー

反応式

HRID 1019660 の反応式
[CH3:1][CH:2]1[NH:7][CH2:6][CH:5]([C:8]([OH:10])=[O:9])[CH2:4][CH2:3]1.Cl.[OH-].[Na+].[CH3:14][CH2:15]O>O>[CH3:1][CH:2]1[NH:7][CH2:6][CH:5]([C:8]([O:10][CH2:14][CH3:15])=[O:9])[CH2:4][CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 14798Sodium HydroxideHCID 136586116-Methylpiperidine-3-carboxylic acid

生成物 1

HCID 13658605Ethyl 6-methylpiperidine-3-carboxylate

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To 194.1 (1044 mg, 7.29 mmol) in EtOH (5207 μL) was added concentrated hydrochloric acid (405 μL, 7.29 mmol). The resulting solution was heated at reflux for 18 hours. The reaction mixture was then cooled to room temperature and poured onto water. The reaction was brought to pH 10 with 1N sodium hydroxide in water and was then extracted with EtOAc. The organic phase was then dried over anhydrous Na2SO4 and filtered to provide ethyl 6-methylpiperidine-3-carboxylate. ESI-MS M+H 172.2.

後処理

  1. temperatureThe resulting solution was heated
  2. temperatureat reflux for 18 hours
  3. additionpoured onto water
  4. extractionwas then extracted with EtOAc
  5. dry with materialThe organic phase was then dried over anhydrous Na2SO4
  6. filtrationfiltered

出典と根拠

ORDレコード
ord-0bb690bac5c14fe995633729d8984e73
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08716281B2

反応ノート

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